Variant (rsID / SNP)
rs10734123
rs10734123 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAALAD2. Location: chromosome 11, position 89,868,755. The table records no clinical significance for this variant.
Reference-table entries
NAALAD2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:89868755
- HGVS
- NM_005467.4,c.111G>A,p.Thr37Thr
- Allele change
- Synonymous_T37T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.